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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5379182translocation1nstd200human GRCh38 chr8: 27,612,232-27,612,232 , GRCh38 chr8: 27,605,408-27,605,408 , GRCh37.p13 chr8: 27,462,925-27,462,925 , GRCh37.p13 chr8: 27,469,749-27,469,749 CLU
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC101929400, LOC105377785, 794 more genes
    nsv4959850copy number variation1nstd200human GRCh38 chr8: 27,579,567-27,596,605 , GRCh37.p13 chr8: 27,437,084-27,454,122 EPHX2, CLU, 1 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 ADRA1A, ADRB3, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 ADRA1A, ADRB3, 411 more genes
    nsv4729723copy number variation1nstd102humanUncertain significance GRCh37 chr8: 27,417,421-27,643,275 , GRCh38.p12 chr8: 27,559,904-27,785,758 CCDC25, RNU6-1086P, 10 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 284 more genes
    nsv4675292copy number variation1nstd102humanPathogenic GRCh37 chr8: 24,305,969-28,673,405 , GRCh38.p12 chr8: 24,448,456-28,815,888 LOC112268023, GNRH1, 80 more genes
    nsv4349554copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 RNU6-1040P, LOC101927513, 2159 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 358 more genes
    nsv4163304copy number variation1nstd166human GRCh37.p13 chr8: 27,437,085-27,454,116 , GRCh38.p12 chr8: 27,579,568-27,596,599 EPHX2, GULOP, 1 more genes
    nsv3972390copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,556,004-34,374,150 , GRCh38.p12 chr8: 12,698,495-34,516,632 NAT1, NAT2, 350 more genes
    nsv3924532copy number variation1nstd102humanPathogenic NCBI36 chr8: 181,605-31,068,132 , GRCh38 chr8: 241,605-31,091,074 , GRCh37 chr8: 191,605-30,948,590 SINHCAFP3, LOC105379350, 604 more genes
    nsv3923600copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,284,724-28,539,000 , GRCh37 chr8: 12,240,353-28,483,081 , GRCh38 chr8: 12,382,844-28,625,564 PIWIL2-DT, MIR6876, 271 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 IQANK1, RPL31P40, 2159 more genes
    nsv3923302copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,210,737 , NCBI36 chr8: 24,823,781-31,187,795 , GRCh37 chr8: 24,767,877-31,068,253 BNIP3L, RBPMS, 125 more genes
    nsv3923174copy number variation1nstd102humanPathogenic GRCh38 chr8: 18,972,996-33,619,264 , GRCh37 chr8: 18,830,506-33,476,782 , NCBI36 chr8: 18,874,786-33,596,324 CHRNA2, LOC102723395, 273 more genes
    nsv3922931copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,383,584-36,370,018 , NCBI36 chr8: 12,285,464-36,347,088 , GRCh37 chr8: 12,241,093-36,227,536 COX6B1P4, LOC105379358, 377 more genes
    nsv3921773copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,511,855-43,310,472 , GRCh38 chr8: 12,609,975-43,336,172 , GRCh37 chr8: 12,467,484-43,191,315 RNU4-71P, POLB, 499 more genes
    nsv3921539copy number variation1nstd102humanPathogenic NCBI36 chr8: 153,682-47,058,107 , GRCh37.p13 chr8: 163,682-46,938,942 , GRCh38.p12 chr8: 213,682-46,027,320 RPL9P20, LOC105379340, 794 more genes
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